Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_02345
Species: Homo sapiens
Position : chr6:12826550-12826620
Year: 2015
Title: Myocardial Infarction-Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary Arteries.
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Disease
Disease Name: coronary artery disease
PMID:  25838425
Tissue: aorta
Tissue Ontology ID: UBERON:0000947
Cell Source: hESC-derived endothelial cells
Cell Type: endothelial cell
Cell Ontology ID: CL:0000115
Experiment Type: Enhancer activity assay, TF binding assay, Functional perturbation assay; Endogenous enhancer perturbation; Disease-variant functional analysis
High Throughput Method: eQTL analysis; GWAS
Low Throughput Method: EMSA, CRISPR knockout, RT-RT-qPCR; CRISPR-Cas9 endogenous deletion/editing
About Target Gene
Target gene : PHACTR1
About TF
TF name : MEF2A
About Regulatory State
Regulatory State : Repressed
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
MEF2A CDO in myogenesis reactome 29
MEF2A ERK/MAPK targets reactome 17
MEF2A Signaling mediated by p38-alpha and p38-beta pid 35
MEF2A TGF_beta_Receptor netpath 220
MEF2A Hs_p38_MAPK_Signaling_Pathway_WP400_72084 wikipathways 28
Enhancer Associated Network
Overlapping Enhancers (hg19) 1 found
Enhancer ID Position Tissue Cell Disease
E_02301 chr6:12826550-12826620 coronary artery endothelial cell myocardial infarction
Expression of Target Genes for the Enhancer